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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1292787Erstellt: 25. Oktober 2026

Water → (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol

https://huagongshe.com/reaction/1292787

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl AcetateHCID 8857—
Edukt5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehydeHCID 1479052—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanolHCID 1786291299,9%

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

A solution of 0.21 g (5.5 mmoles) of lithium aluminum hydride dissolved in 70 ml of THF was cooled to -30° C. Thereto was gradually added a solution of 3 g (10.9 mmoles) of 5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4carboaldehyde dissolved in 30 ml of tetrahydrofuran. The resulting mixture was stirred at −30° C. for 30 minutes to give rise to a reaction. After the completion of the reaction, ethyl acetate was added, followed by stirring. Then, water was added, followed by stirring for a while. The reaction mixture was filtered under vacuum. The filtrate was extracted with ethyl acetate. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 3.0 g (yield: 99.9%) of (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol as white crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07238689B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-f1fdcb4890e740d6a96071ffc74dd11b
Quellennotizuspto-grants-2007_07